[PMID 17048007] Association of warfarin dose with genes involved in its action and metabolism.

rs6583954

Parent Gene: CYP2C19

Importance: 3
Less common allele: T = 23%
More common allele: C = 77%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Migraine Disorder

The T allele of rs6583954 is reported to be associated with Migraine Disorder (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Migraine.